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Sign in to claim this brandMidmark Corporation
United States·US-MF-000002581
Last updated September 17, 2026
About
Midmark is a global manufacturer and supplier of healthcare products, equipment and diagnostic software for medical, veterinary, and dental markets.
From the manufacturer's own website. Source
Information
- Country
- United States
- Address
- 60, Vista Drive, Versailles, United States
- Website
- www.midmark.com
- facebook.com/MidmarkCorporation
- [email protected]
- Phone
- —
- PRRC Contact
- Adam Clutter
- EUDAMED SRN
- US-MF-000002581
- FDA FEI Number
- 1523530
- DUNS Number
- —
Catalogue (1527)
Page 6 of 31| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Midmark PREVA IntraOral Dental X-ray System | DCD6-G2N/S2 | FDA UDI | Class II | Active |
| Midmark VETPRO IntraOral Dental X-ray System | DCV7-G1A/H/SC | FDA UDI | Class II | Active |
| Ritter | 9A328001 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6DE-W1Y/H/S1 | FDA UDI | N/A | Active |
| Midmark | DCD7-G2Z | FDA UDI | Class II | Active |
| Midmark | DCV7-G2X/H/SB | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCDM-W0Z/H/SB | FDA UDI | Class II | Active |
| Midmark OptiMax Digital Sensor System | XSVQ-04 | FDA UDI | Class II | Active |
| Ritter | 253-012 | FDA UDI | Class I | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6-W2B/S1 | FDA UDI | Class II | Active |
| Ritter | 255-007 | FDA UDI | Class I | Active |
| Midmark PREVA 2.0 IntraOral Dental X-ray System | DCD5-W2B | FDA UDI | Class II | Active |
| Midmark Extraoral Imaging System (EOIS) | 60-A0012 / 60-A0015 | FDA UDI | Class II | Active |
| Midmark | DCD5-G2Z/S1 | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD5‐G2N/S1 | FDA UDI | Class II | Active |
| Midmark | 1531018-016 | FDA UDI | Class I | Active |
| Ritter | 230-002 | FDA UDI | Class I | Active |
| Midmark | 9A496001-864 | FDA UDI | Class I | Active |
| Midmark | 9A378001-855 | FDA UDI | Class I | Active |
| Midmark | 153592-005 | FDA UDI | Class I | Active |
| Midmark | DCD7-G1Z/S2 | FDA UDI | Class II | Active |
| Midmark | 153604LRCA-E | FDA UDI | Class I | Active |
| Ritter | 253-016 | FDA UDI | Class I | Active |
| Midmark | 9A378001-859 | FDA UDI | Class I | Active |
| Ritter | 9A51001-853 | FDA UDI | Class I | Active |
| Midmark | 153829-001 | FDA UDI | Class I | Unknown |
| Midmark OptiMax Digital Sensor System | XSVS-04/L | FDA UDI | Class II | Active |
| Midmark | DCV7-G1X/H/S4 | FDA UDI | Class II | Active |
| Midmark OptiMax Digital Sensor System | XSVN-03/L | FDA UDI | Class II | Active |
| Midmark Intraoral Digital Sensor | XSDS-0D/L | FDA UDI | Class II | Active |
| Midmark | DCD7-G1Z/SB | FDA UDI | Class II | Active |
| Midmark PREVA IntraOral Dental X-ray System | DCD6DE-W1X/H/S1 | FDA UDI | Class II | Active |
| Midmark | DCD5-G2Z | FDA UDI | Class II | Active |
| Ritter | 9A337001-850 | FDA UDI | Class I | Active |
| Midmark | 9A739001-857 | FDA UDI | Class I | Active |
| Midmark | 9A386001-845 | FDA UDI | Class I | Active |
| Ritter M9 Ultraclave | M9D-022 | FDA UDI | Class II | Active |
| Midmark | 9A382001-232 | FDA UDI | Class I | Active |
| Midmark ClearVision Digital Sensor System with Laptop | XSDN-02/L | FDA UDI | Class II | Active |
| Midmark | 9A684001-813 | FDA UDI | Class I | Active |
| Midmark | XSVN-01/L | FDA UDI | Class II | Active |
| M11 Ultraclave | M11-021 | FDA UDI | Class II | Active |
| Midmark | 153901-007 | FDA UDI | Class I | Active |
| Midmark | 9A390001-863 | FDA UDI | Class I | Active |
| Midmark | 9A684001-232 | FDA UDI | Class I | Active |
| Midmark | DCV8-G2X/H | FDA UDI | Class II | Active |
| Midmark | DCD6-G2Z/S2 | FDA UDI | Class II | Active |
| Ritter | 9A621001 | FDA UDI | Class I | Active |
| M11 Vertical Cassette Rack | 9A215002 | FDA UDI | Class II | Active |
| Midmark | P22SC/CV3R | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
- CEpartner4U NL
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 5, 2003 | Z-0704-03 | — | terminated | The pressure relief valve may fail to open properly. |